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Artigo de periodico-dep/entr
Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário] (2015)
Santos, Raul D.; Watts, Gerald F.
Source: Lancet. Unidade: FM
Subjects: FATORES DE RISCO, MUTAÇÃO GENÉTICA, DOENÇAS CARDIOVASCULARES (ETIOLOGIA), HIPERCOLESTEROLEMIA (COMPLICAÇÕES)
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ABNT
SANTOS, Raul D. e WATTS, Gerald F. Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário]. Lancet. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/S0140-6736(14)61702-5. Acesso em: 28 jun. 2024. , 2015
APA
Santos, R. D., & Watts, G. F. (2015). Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário]. Lancet. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/S0140-6736(14)61702-5
NLM
Santos RD, Watts GF. Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário] [Internet]. Lancet. 2015 ; 385( 9965): 307-310.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/S0140-6736(14)61702-5
Vancouver
Santos RD, Watts GF. Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário] [Internet]. Lancet. 2015 ; 385( 9965): 307-310.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/S0140-6736(14)61702-5
Artigo de periodico
The presence of resistance mutations to protease and polymerase inhibitors in Hepatitis C virus sequences from the Los Alamos databank (2013)
Alves, R.; Queiroz, A. T. L.; Pessoa, M. G.; Silva, E. F. da; Mazo, D. F. C.; Carrilho, F. J.; Carvalho-Filho, R. J.; Carvalho, I. M. V. G. de
Source: Journal of Viral Hepatitis. Unidade: FM
Subjects: VÍRUS DA HEPATITE C, MUTAÇÃO GENÉTICA, REAÇÃO EM CADEIA POR POLIMERASE, GENÓTIPOS, ANTIVIRAIS (RESISTÊNCIA)
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ABNT
ALVES, R. et al. The presence of resistance mutations to protease and polymerase inhibitors in Hepatitis C virus sequences from the Los Alamos databank. Journal of Viral Hepatitis, v. 20, n. 6, p. 414-421, 2013Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/jvh.12051/pdf. Acesso em: 28 jun. 2024.
APA
Alves, R., Queiroz, A. T. L., Pessoa, M. G., Silva, E. F. da, Mazo, D. F. C., Carrilho, F. J., et al. (2013). The presence of resistance mutations to protease and polymerase inhibitors in Hepatitis C virus sequences from the Los Alamos databank. Journal of Viral Hepatitis, 20( 6), 414-421. doi:10.1111/jvh.12051
NLM
Alves R, Queiroz ATL, Pessoa MG, Silva EF da, Mazo DFC, Carrilho FJ, Carvalho-Filho RJ, Carvalho IMVG de. The presence of resistance mutations to protease and polymerase inhibitors in Hepatitis C virus sequences from the Los Alamos databank [Internet]. Journal of Viral Hepatitis. 2013 ; 20( 6): 414-421.[citado 2024 jun. 28 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/jvh.12051/pdf
Vancouver
Alves R, Queiroz ATL, Pessoa MG, Silva EF da, Mazo DFC, Carrilho FJ, Carvalho-Filho RJ, Carvalho IMVG de. The presence of resistance mutations to protease and polymerase inhibitors in Hepatitis C virus sequences from the Los Alamos databank [Internet]. Journal of Viral Hepatitis. 2013 ; 20( 6): 414-421.[citado 2024 jun. 28 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/jvh.12051/pdf
Artigo de periodico
Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years (2012)
Lima, Hildenêr Nogueira; Botosso, Viviane Fongaro; Oliveira, Danielle Bruna Leal; Campos, Angélica Cristine de Almeida; Leal, Andrea Lima; Silva, Tereza Souza; Bosso, Patrícia Alves Ramos; Moraes, Claudia Trigo Pedroso; Silva Filho, Claudionor Gomes da; Vieira, Sandra Elisabete; Gilio, Alfredo Elias; Stewien, Klaus Eberhard; Durigon, Edison Luiz
Source: Virus Research. Unidades: FM, ICB
Subjects: GENES (ANÁLISE), DOENÇAS RESPIRATÓRIAS, PROTEÍNAS, NASOFARINGE (SECREÇÃO), APOPTOSE, VARIAÇÃO GENÉTICA, HOSPEDEIRO IMUNOCOMPROMETIDO, GENÓTIPOS, MUTAÇÃO GENÉTICA
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ABNT
LIMA, Hildenêr Nogueira et al. Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years. Virus Research, v. 163, n. 1, p. 82-86, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.virusres.2011.08.013. Acesso em: 28 jun. 2024.
APA
Lima, H. N., Botosso, V. F., Oliveira, D. B. L., Campos, A. C. de A., Leal, A. L., Silva, T. S., et al. (2012). Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years. Virus Research, 163( 1), 82-86. doi:10.1016/j.virusres.2011.08.013
NLM
Lima HN, Botosso VF, Oliveira DBL, Campos AC de A, Leal AL, Silva TS, Bosso PAR, Moraes CTP, Silva Filho CG da, Vieira SE, Gilio AE, Stewien KE, Durigon EL. Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years [Internet]. Virus Research. 2012 ; 163( 1): 82-86.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.virusres.2011.08.013
Vancouver
Lima HN, Botosso VF, Oliveira DBL, Campos AC de A, Leal AL, Silva TS, Bosso PAR, Moraes CTP, Silva Filho CG da, Vieira SE, Gilio AE, Stewien KE, Durigon EL. Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years [Internet]. Virus Research. 2012 ; 163( 1): 82-86.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.virusres.2011.08.013
Artigo de periodico
Deregulated expression of A1, Bcl-2, Bcl-xL, and Mcl-1 antiapoptotic proteins and Bid, Bad, and Bax proapoptotic genes in polycythemia vera patients (2011)
Gasparotto, Elainy Patricia Lino; Tognon, Raquel; Ferreira, Aline Fernanda; Oliveira, Gislane Lelis Vilela; Palma, Patrícia Vianna Bonini; Zanichelli, Maria Aparecida; Souto, Elizabeth Xisto; Velano, Carlos Eduardo Engel; Simoes, Belinda Pinto; Carrara, Rita de Cassia Viu; Kashima, Simone; Covas, Dimas Tadeu; Castro, Fabíola Attié de; Souza, Ana Maria de
Source: BJPS - Brazilian Journal of Pharmaceutical Sciences. Unidades: FMRP, FCFRP
Subjects: POLICITEMIA, MUTAÇÃO GENÉTICA, EXPRESSÃO GÊNICA, APOPTOSE
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ABNT
GASPAROTTO, Elainy Patricia Lino et al. Deregulated expression of A1, Bcl-2, Bcl-xL, and Mcl-1 antiapoptotic proteins and Bid, Bad, and Bax proapoptotic genes in polycythemia vera patients. BJPS - Brazilian Journal of Pharmaceutical Sciences, v. 47, n. 4, p. 873-884, 2011Tradução . . Disponível em: https://doi.org/10.1590/S1984-82502011000400025. Acesso em: 28 jun. 2024.
APA
Gasparotto, E. P. L., Tognon, R., Ferreira, A. F., Oliveira, G. L. V., Palma, P. V. B., Zanichelli, M. A., et al. (2011). Deregulated expression of A1, Bcl-2, Bcl-xL, and Mcl-1 antiapoptotic proteins and Bid, Bad, and Bax proapoptotic genes in polycythemia vera patients. BJPS - Brazilian Journal of Pharmaceutical Sciences, 47( 4), 873-884. doi:10.1590/S1984-82502011000400025
NLM
Gasparotto EPL, Tognon R, Ferreira AF, Oliveira GLV, Palma PVB, Zanichelli MA, Souto EX, Velano CEE, Simoes BP, Carrara R de CV, Kashima S, Covas DT, Castro FA de, Souza AM de. Deregulated expression of A1, Bcl-2, Bcl-xL, and Mcl-1 antiapoptotic proteins and Bid, Bad, and Bax proapoptotic genes in polycythemia vera patients [Internet]. BJPS - Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47( 4): 873-884.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/S1984-82502011000400025
Vancouver
Gasparotto EPL, Tognon R, Ferreira AF, Oliveira GLV, Palma PVB, Zanichelli MA, Souto EX, Velano CEE, Simoes BP, Carrara R de CV, Kashima S, Covas DT, Castro FA de, Souza AM de. Deregulated expression of A1, Bcl-2, Bcl-xL, and Mcl-1 antiapoptotic proteins and Bid, Bad, and Bax proapoptotic genes in polycythemia vera patients [Internet]. BJPS - Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47( 4): 873-884.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/S1984-82502011000400025
Artigo de periodico
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency (2011)
França, Marcela M.; Jorge, Alexander A. L.; Alatzoglou, Kyriaki S.; Carvalho, Luciani R. S.; Mendonça, Berenice Bilharinho; Audi, Laura; Carrascosa, Antonio; Dattani, Mehul T.; Arnhold, Ivo J. P.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), FENÓTIPOS, ELETROFORESE, SEGUIMENTO GENÉTICO
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ABNT
FRANÇA, Marcela M. et al. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 9, p. E1457-1460, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-0170. Acesso em: 28 jun. 2024.
APA
França, M. M., Jorge, A. A. L., Alatzoglou, K. S., Carvalho, L. R. S., Mendonça, B. B., Audi, L., et al. (2011). Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency. Journal of Clinical Endocrinology and Metabolism, 96( 9), E1457-1460. doi:10.1210/jc.2011-0170
NLM
França MM, Jorge AAL, Alatzoglou KS, Carvalho LRS, Mendonça BB, Audi L, Carrascosa A, Dattani MT, Arnhold IJP. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 9): E1457-1460.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2011-0170
Vancouver
França MM, Jorge AAL, Alatzoglou KS, Carvalho LRS, Mendonça BB, Audi L, Carrascosa A, Dattani MT, Arnhold IJP. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 9): E1457-1460.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2011-0170
Artigo de periodico
TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood (2010)
Gianetti, Elena; Tusset, Cintia; Noel, Sekoni D.; Au, Margaret G.; Dwyer, Andrew A.; Hughes, Virginia A.; Abreu, Ana Paula; Carroll, Jessica; Trarbach, Ericka; Silveira, Leticia F. G.; Costa, Elaine M. F.; Mendonça, Berenice Bilharinho de; Castro, Margaret de; Lofrano, Adriana; Hall, Janet E.; Bolu, Erol; Ozata, Metin; Quinton, Richard; Amory, John K.; Stewart, Susan E.; Arlt, Wiebke; Cole, Trevor R.; Crowley, William F.; Kaiser, Ursula B.; Latronico, Ana Claudia; Seminara, Stephanie B.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), GONADOTROFINAS (METABOLISMO), FENÓTIPOS, HIPOGONADISMO
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ABNT
GIANETTI, Elena et al. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 5, p. 2857-2867, 2010Tradução . . Disponível em: https://doi.org/10.1210/jc.2009-2320. Acesso em: 28 jun. 2024.
APA
Gianetti, E., Tusset, C., Noel, S. D., Au, M. G., Dwyer, A. A., Hughes, V. A., et al. (2010). TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood. Journal of Clinical Endocrinology and Metabolism, 95( 5), 2857-2867. doi:10.1210/jc.2009-2320
NLM
Gianetti E, Tusset C, Noel SD, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carroll J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB de, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser UB, Latronico AC, Seminara SB. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2857-2867.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2009-2320
Vancouver
Gianetti E, Tusset C, Noel SD, Au MG, Dwyer AA, Hughes VA, Abreu AP, Carroll J, Trarbach E, Silveira LFG, Costa EMF, Mendonça BB de, Castro M de, Lofrano A, Hall JE, Bolu E, Ozata M, Quinton R, Amory JK, Stewart SE, Arlt W, Cole TR, Crowley WF, Kaiser UB, Latronico AC, Seminara SB. TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2857-2867.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2009-2320
Artigo de periodico
Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction (2010)
Silveira, Leticia Gontijo; Tusset, Cintia; Xavier, Ana Claudia Latronico
Source: Brain research. Unidade: FM
Subjects: REPRODUÇÃO, HIPOGONADISMO, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
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ABNT
SILVEIRA, Leticia Gontijo e TUSSET, Cintia e XAVIER, Ana Claudia Latronico. Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction. Brain research, v. 1364, p. 72-80, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.brainres.2010.08.087. Acesso em: 28 jun. 2024.
APA
Silveira, L. G., Tusset, C., & Xavier, A. C. L. (2010). Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction. Brain research, 1364, 72-80. doi:10.1016/j.brainres.2010.08.087
NLM
Silveira LG, Tusset C, Xavier ACL. Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction [Internet]. Brain research. 2010 ; 1364 72-80.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.brainres.2010.08.087
Vancouver
Silveira LG, Tusset C, Xavier ACL. Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction [Internet]. Brain research. 2010 ; 1364 72-80.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.brainres.2010.08.087
Artigo de periodico
Clinical and molecular characterization of Brazilian familie4s with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation (2010)
Gomy, Israel; Molfetta, Greice Andreotti de; Barreto, Ester de Andrade; Ferreira, Cristiane Ayres; Zanette, Dalila Luciola; Rocha, José Cláudio Casali da; Silva Júnior, Wilson Araújo da
Source: Familial Cancer. Unidade: FMRP
Subjects: NEOPLASIAS, MUTAÇÃO GENÉTICA
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ABNT
GOMY, Israel et al. Clinical and molecular characterization of Brazilian familie4s with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation. Familial Cancer, v. 0, n. 4, p. 635-642, 2010Tradução . . Disponível em: https://doi.org/10.1007/s10689-010-9357-2. Acesso em: 28 jun. 2024.
APA
Gomy, I., Molfetta, G. A. de, Barreto, E. de A., Ferreira, C. A., Zanette, D. L., Rocha, J. C. C. da, & Silva Júnior, W. A. da. (2010). Clinical and molecular characterization of Brazilian familie4s with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation. Familial Cancer, 0( 4), 635-642. doi:10.1007/s10689-010-9357-2
NLM
Gomy I, Molfetta GA de, Barreto E de A, Ferreira CA, Zanette DL, Rocha JCC da, Silva Júnior WA da. Clinical and molecular characterization of Brazilian familie4s with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation [Internet]. Familial Cancer. 2010 ; 0( 4): 635-642.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s10689-010-9357-2
Vancouver
Gomy I, Molfetta GA de, Barreto E de A, Ferreira CA, Zanette DL, Rocha JCC da, Silva Júnior WA da. Clinical and molecular characterization of Brazilian familie4s with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation [Internet]. Familial Cancer. 2010 ; 0( 4): 635-642.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s10689-010-9357-2
Artigo de periodico
Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study (2010)
Daly, Adrian F.; Tichomirowa, Maria A.; Petrossians, Patrick; Heliövaara, Elina; Jaffrain-Rea, Marie-Lise; Barlier, Anne; Naves, Luciana A.; Ebeling, Tapani; Karhu, Auli; Raappana, Antti; Cazabat, Laure; De Menis, Ernesto; Montañana, Carmen Fajardo; Raverot, Gerald; Weil, Robert J.; Sane, Timo; Maiter, Dominique; Neggers, Sebastian; Yaneva, Maria; Tabarin, AntoineAntoine; Verrua, Elisa; Eloranta, Eija; Murat, Arnaud; Vierimaa, Outi; Salmela, Pasi I.; Emy, Philippe; Toledo, Rodrigo A.; Sabaté , Maria Isabel; Villa, Chiara; Popelier, Marc; Salvatori, Roberto; Jennings, Juliet; Longás, Ángel Ferrandez; Aizpún, José Ignacio Labarta; Georgitsi, Marianthi; Paschke, Ralf; Ronchi, Cristina; Valimaki, Matti; Saloranta, Carola; De Herder, Wouter; Cozzi, Renato; Guitelman, Mirtha; Magri, Flavia; Lagonigro, Maria Stefania; Halaby, Georges; Corman, Vinciane; Hagelstein, Marie-Thérèse; Vanbellinghen, Jean-Francis; Barra, Gustavo Barcelos; Gimenez-Roqueplo, Anne-Paule; Cameron, Fergus J.; Borson-Chazot, Francoise; Holdaway, Ian; Toledo, Sergio P. A.; Stalla, Gunter K.; Spada, Anna; Zacharieva, Sabina; Bertherat, Jerome; Brue, Thierry; Bours, Vincent; Chanson, Philippe; Aaltonen, Lauri A.; Beckers, Albert
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, ESTUDOS RETROSPECTIVOS, GLÂNDULA PRITUITÁRIA (PATOLOGIA), ADENOMAS (PATOLOGIA)
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ABNT
DALY, Adrian F. et al. Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 11, p. E373-E383, 2010Tradução . . Disponível em: https://doi.org/10.1210/jc.2009-2556. Acesso em: 28 jun. 2024.
APA
Daly, A. F., Tichomirowa, M. A., Petrossians, P., Heliövaara, E., Jaffrain-Rea, M. -L., Barlier, A., et al. (2010). Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study. Journal of Clinical Endocrinology and Metabolism, 95( 11), E373-E383. doi:10.1210/jc.2009-2556
NLM
Daly AF, Tichomirowa MA, Petrossians P, Heliövaara E, Jaffrain-Rea M-L, Barlier A, Naves LA, Ebeling T, Karhu A, Raappana A, Cazabat L, De Menis E, Montañana CF, Raverot G, Weil RJ, Sane T, Maiter D, Neggers S, Yaneva M, Tabarin AA, Verrua E, Eloranta E, Murat A, Vierimaa O, Salmela PI, Emy P, Toledo RA, Sabaté MI, Villa C, Popelier M, Salvatori R, Jennings J, Longás ÁF, Aizpún JIL, Georgitsi M, Paschke R, Ronchi C, Valimaki M, Saloranta C, De Herder W, Cozzi R, Guitelman M, Magri F, Lagonigro MS, Halaby G, Corman V, Hagelstein M-T, Vanbellinghen J-F, Barra GB, Gimenez-Roqueplo A-P, Cameron FJ, Borson-Chazot F, Holdaway I, Toledo SPA, Stalla GK, Spada A, Zacharieva S, Bertherat J, Brue T, Bours V, Chanson P, Aaltonen LA, Beckers A. Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 11): E373-E383.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2009-2556
Vancouver
Daly AF, Tichomirowa MA, Petrossians P, Heliövaara E, Jaffrain-Rea M-L, Barlier A, Naves LA, Ebeling T, Karhu A, Raappana A, Cazabat L, De Menis E, Montañana CF, Raverot G, Weil RJ, Sane T, Maiter D, Neggers S, Yaneva M, Tabarin AA, Verrua E, Eloranta E, Murat A, Vierimaa O, Salmela PI, Emy P, Toledo RA, Sabaté MI, Villa C, Popelier M, Salvatori R, Jennings J, Longás ÁF, Aizpún JIL, Georgitsi M, Paschke R, Ronchi C, Valimaki M, Saloranta C, De Herder W, Cozzi R, Guitelman M, Magri F, Lagonigro MS, Halaby G, Corman V, Hagelstein M-T, Vanbellinghen J-F, Barra GB, Gimenez-Roqueplo A-P, Cameron FJ, Borson-Chazot F, Holdaway I, Toledo SPA, Stalla GK, Spada A, Zacharieva S, Bertherat J, Brue T, Bours V, Chanson P, Aaltonen LA, Beckers A. Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 11): E373-E383.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2009-2556
Artigo de periodico
Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes (2010)
Gouvêa, Silmara P.; Borghetti, Vinicius Horacio Stefani; Bueno, Keity Cristina; Genari, Adriana Borges; Lourenço, Charles Marques; Sobreira, Cláudia Ferreira da Rosa; Barreira, Amilton Antunes; Marques Júnior, Wilson
Source: Neurogenetics. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, DOENÇAS DO SISTEMA NERVOSO
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ABNT
GOUVÊA, Silmara P. et al. Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes. Neurogenetics, v. 11, n. 1, p. 135-138, 2010Tradução . . Disponível em: https://doi.org/10.1007/s10048-009-0211-3. Acesso em: 28 jun. 2024.
APA
Gouvêa, S. P., Borghetti, V. H. S., Bueno, K. C., Genari, A. B., Lourenço, C. M., Sobreira, C. F. da R., et al. (2010). Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes. Neurogenetics, 11( 1), 135-138. doi:10.1007/s10048-009-0211-3
NLM
Gouvêa SP, Borghetti VHS, Bueno KC, Genari AB, Lourenço CM, Sobreira CF da R, Barreira AA, Marques Júnior W. Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes [Internet]. Neurogenetics. 2010 ; 11( 1): 135-138.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s10048-009-0211-3
Vancouver
Gouvêa SP, Borghetti VHS, Bueno KC, Genari AB, Lourenço CM, Sobreira CF da R, Barreira AA, Marques Júnior W. Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes [Internet]. Neurogenetics. 2010 ; 11( 1): 135-138.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s10048-009-0211-3
Artigo de periodico
Mutations of the KISS1 gene in disorders of puberty (2010)
Silveira, L. G.; Noel, S. D.; Silveira-Neto, A. P.; Abreu, A. P.; Brito, V. N.; Santos, M. G; Bianco, S. D. C.; Kuohung, W.; Xu, S.; Gryngarten, M.; Escobar, M. E.; Arnhold, I. J. P.; Mendonca, B. B.; Kaiser, U. B.; Latronico, A. C.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENES (ANÁLISE), PUBERDADE (GENÉTICA), FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, L. G. et al. Mutations of the KISS1 gene in disorders of puberty. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 5, p. 2276-2280, 2010Tradução . . Disponível em: http://jcem.endojournals.org/cgi/reprint/95/5/2276. Acesso em: 28 jun. 2024.
APA
Silveira, L. G., Noel, S. D., Silveira-Neto, A. P., Abreu, A. P., Brito, V. N., Santos, M. G., et al. (2010). Mutations of the KISS1 gene in disorders of puberty. Journal of Clinical Endocrinology and Metabolism, 95( 5), 2276-2280. Recuperado de http://jcem.endojournals.org/cgi/reprint/95/5/2276
NLM
Silveira LG, Noel SD, Silveira-Neto AP, Abreu AP, Brito VN, Santos MG, Bianco SDC, Kuohung W, Xu S, Gryngarten M, Escobar ME, Arnhold IJP, Mendonca BB, Kaiser UB, Latronico AC. Mutations of the KISS1 gene in disorders of puberty [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2276-2280.[citado 2024 jun. 28 ] Available from: http://jcem.endojournals.org/cgi/reprint/95/5/2276
Vancouver
Silveira LG, Noel SD, Silveira-Neto AP, Abreu AP, Brito VN, Santos MG, Bianco SDC, Kuohung W, Xu S, Gryngarten M, Escobar ME, Arnhold IJP, Mendonca BB, Kaiser UB, Latronico AC. Mutations of the KISS1 gene in disorders of puberty [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 5): 2276-2280.[citado 2024 jun. 28 ] Available from: http://jcem.endojournals.org/cgi/reprint/95/5/2276
Artigo de periodico
The H63D genetic variant of the HFE gene is independently associated with the virological response to interferon and ribavirin therapy in chronic hepatitis C (2010)
Carneiro, Marcos de Vanconcelos; Souza, Fernanda Fernandes; Teixeira, Andreza Correa; Figueiredo, José Fernando de Castro; Villanova, Marcia Guimaraes; Secaf, Marie; Passos, Afonso Dinis Costa; Ramalho, Leandra Naíra Zambelli; Carneiro, Fabiana Pirani; Zucoloto, Sergio; Martinelli, Ana de Lourdes Candolo
Source: European Journal of Gastroenterology and Hepatology. Unidade: FMRP
Subjects: HEPATITE C, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARNEIRO, Marcos de Vanconcelos et al. The H63D genetic variant of the HFE gene is independently associated with the virological response to interferon and ribavirin therapy in chronic hepatitis C. European Journal of Gastroenterology and Hepatology, v. 22, n. 10, p. 1204-1210, 2010Tradução . . Disponível em: https://doi.org/10.1097/meg.0b013e32833bec1e. Acesso em: 28 jun. 2024.
APA
Carneiro, M. de V., Souza, F. F., Teixeira, A. C., Figueiredo, J. F. de C., Villanova, M. G., Secaf, M., et al. (2010). The H63D genetic variant of the HFE gene is independently associated with the virological response to interferon and ribavirin therapy in chronic hepatitis C. European Journal of Gastroenterology and Hepatology, 22( 10), 1204-1210. doi:10.1097/meg.0b013e32833bec1e
NLM
Carneiro M de V, Souza FF, Teixeira AC, Figueiredo JF de C, Villanova MG, Secaf M, Passos ADC, Ramalho LNZ, Carneiro FP, Zucoloto S, Martinelli A de LC. The H63D genetic variant of the HFE gene is independently associated with the virological response to interferon and ribavirin therapy in chronic hepatitis C [Internet]. European Journal of Gastroenterology and Hepatology. 2010 ; 22( 10): 1204-1210.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1097/meg.0b013e32833bec1e
Vancouver
Carneiro M de V, Souza FF, Teixeira AC, Figueiredo JF de C, Villanova MG, Secaf M, Passos ADC, Ramalho LNZ, Carneiro FP, Zucoloto S, Martinelli A de LC. The H63D genetic variant of the HFE gene is independently associated with the virological response to interferon and ribavirin therapy in chronic hepatitis C [Internet]. European Journal of Gastroenterology and Hepatology. 2010 ; 22( 10): 1204-1210.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1097/meg.0b013e32833bec1e
Artigo de periodico
Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations (2009)
Oba-Shinjo, Sueli M.; Basso-Silva, Roseli ; Andrade, Fernanda G.; Palmer, Rachel E.; Pomponio, Robert J.; Ciociola, Kristina M.; Carvalho, Mary S.; Gutierrez, Paulo S.; Porta, Gilda; Marrone, Carlo D.; Munoz, Verônica; Grzesiuk, Anderson K.; Llerena Júnior, Juan C.; Berditchevsky, Célia R.; Sobreira, Cláudia Ferreira da Rosa; Horovitz, Dafne; Hatem, Thamine P.; Frota, Elizabeth Regina Comini; Pecchini, Rogerio; Kouyoumdjian, João Aris; Werneck, Lineu; Amado, Verônica M.; Camelo Júnior, José Simon; Mattaliano, Robert; Marie, Suely Kazue Nagahashi
Source: Journal of Neurology. Unidades: FM, FEARP, FMRP
Subjects: MUTAÇÃO GENÉTICA, NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OBA-SHINJO, Sueli M. et al. Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations. Journal of Neurology, v. 256, n. 11, p. 1881-1890, 2009Tradução . . Disponível em: https://doi.org/10.1007/s00415-009-5219-y. Acesso em: 28 jun. 2024.
APA
Oba-Shinjo, S. M., Basso-Silva, R., Andrade, F. G., Palmer, R. E., Pomponio, R. J., Ciociola, K. M., et al. (2009). Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations. Journal of Neurology, 256( 11), 1881-1890. doi:10.1007/s00415-009-5219-y
NLM
Oba-Shinjo SM, Basso-Silva R, Andrade FG, Palmer RE, Pomponio RJ, Ciociola KM, Carvalho MS, Gutierrez PS, Porta G, Marrone CD, Munoz V, Grzesiuk AK, Llerena Júnior JC, Berditchevsky CR, Sobreira CF da R, Horovitz D, Hatem TP, Frota ERC, Pecchini R, Kouyoumdjian JA, Werneck L, Amado VM, Camelo Júnior JS, Mattaliano R, Marie SKN. Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations [Internet]. Journal of Neurology. 2009 ; 256( 11): 1881-1890.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s00415-009-5219-y
Vancouver
Oba-Shinjo SM, Basso-Silva R, Andrade FG, Palmer RE, Pomponio RJ, Ciociola KM, Carvalho MS, Gutierrez PS, Porta G, Marrone CD, Munoz V, Grzesiuk AK, Llerena Júnior JC, Berditchevsky CR, Sobreira CF da R, Horovitz D, Hatem TP, Frota ERC, Pecchini R, Kouyoumdjian JA, Werneck L, Amado VM, Camelo Júnior JS, Mattaliano R, Marie SKN. Pompe disease in a Brazilian series:: clinical and molecular analyses with identification of nine new mutations [Internet]. Journal of Neurology. 2009 ; 256( 11): 1881-1890.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1007/s00415-009-5219-y
Artigo de periodico
A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil (2009)
Oliveira, Raimundo Antônio Gomes; Oshiro, Marilena; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Ribeiro, Georgina Severo; Medeiros, Tereza Maria Dantas de; Barretto, Orlando César de Oliveira
Source: Genetics and Molecular Biology. Unidades: FCF, FM
Subjects: POLIMORFISMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Raimundo Antônio Gomes et al. A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil. Genetics and Molecular Biology, 2009Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572009005000033. Acesso em: 28 jun. 2024.
APA
Oliveira, R. A. G., Oshiro, M., Hirata, M. H., Hirata, R. D. C., Ribeiro, G. S., Medeiros, T. M. D. de, & Barretto, O. C. de O. (2009). A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil. Genetics and Molecular Biology. doi:10.1590/s1415-47572009005000033
NLM
Oliveira RAG, Oshiro M, Hirata MH, Hirata RDC, Ribeiro GS, Medeiros TMD de, Barretto OC de O. A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil [Internet]. Genetics and Molecular Biology. 2009 ;[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/s1415-47572009005000033
Vancouver
Oliveira RAG, Oshiro M, Hirata MH, Hirata RDC, Ribeiro GS, Medeiros TMD de, Barretto OC de O. A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil [Internet]. Genetics and Molecular Biology. 2009 ;[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/s1415-47572009005000033
Artigo de periodico
Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course (2009)
Sobreira, Cláudia Ferreira da Rosa; Marques Júnior, Wilson; Pontes-Neto, Octávio Marques; Santos, Antônio Carlos dos; Pina Neto, João Monteiro de; Barreira, Amilton Antunes
Source: Journal of the Neurological Sciences. Unidade: FMRP
Subjects: NEUROLOGIA, MUTAÇÃO GENÉTICA, MITOCÔNDRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOBREIRA, Cláudia Ferreira da Rosa et al. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course. Journal of the Neurological Sciences, v. 278, n. 1-2, p. 132-134, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jns.2008.11.023. Acesso em: 28 jun. 2024.
APA
Sobreira, C. F. da R., Marques Júnior, W., Pontes-Neto, O. M., Santos, A. C. dos, Pina Neto, J. M. de, & Barreira, A. A. (2009). Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course. Journal of the Neurological Sciences, 278( 1-2), 132-134. doi:10.1016/j.jns.2008.11.023
NLM
Sobreira CF da R, Marques Júnior W, Pontes-Neto OM, Santos AC dos, Pina Neto JM de, Barreira AA. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course [Internet]. Journal of the Neurological Sciences. 2009 ; 278( 1-2): 132-134.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.jns.2008.11.023
Vancouver
Sobreira CF da R, Marques Júnior W, Pontes-Neto OM, Santos AC dos, Pina Neto JM de, Barreira AA. Leigh-like syndrome with the T8993G mutation in the mitochondrial ATPase 6 gene: long-term follow-up discloses a slowly progressive course [Internet]. Journal of the Neurological Sciences. 2009 ; 278( 1-2): 132-134.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.jns.2008.11.023
Artigo de periodico
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients (2008)
Raskin, Salmo; Ferrari, Lilian Pereira; Reis, Francisco Caldeira; Abreu, Fernando; Marostica, Paulo; Rozov, Tatiana; Cardieri, Joselina; Ludwing, Norberto; Valentin, Lairton; Rosario Filho, Nelson Augusto; Camargo Neto, Eurico; Lewis, Eduardo; Giugliani, Roberto; Diniz, Edna Maria Albuquerque; Culpi, Lodercio; Phillip III, John Atlas; Chakraborty, Ranajit
Source: Journal of cystic fibrosis. Unidade: FM
Subjects: FIBROSE CÍSTICA (INCIDÊNCIA), RASTREAMENTO, MUTAÇÃO GENÉTICA, RECÉM-NASCIDOS, PACIENTES, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RASKIN, Salmo et al. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. Journal of cystic fibrosis, v. 7, n. 1, p. 15-22, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jcf.2007.03.006. Acesso em: 28 jun. 2024.
APA
Raskin, S., Ferrari, L. P., Reis, F. C., Abreu, F., Marostica, P., Rozov, T., et al. (2008). Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. Journal of cystic fibrosis, 7( 1), 15-22. doi:10.1016/j.jcf.2007.03.006
NLM
Raskin S, Ferrari LP, Reis FC, Abreu F, Marostica P, Rozov T, Cardieri J, Ludwing N, Valentin L, Rosario Filho NA, Camargo Neto E, Lewis E, Giugliani R, Diniz EMA, Culpi L, Phillip III JA, Chakraborty R. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients [Internet]. Journal of cystic fibrosis. 2008 ; 7( 1): 15-22.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.jcf.2007.03.006
Vancouver
Raskin S, Ferrari LP, Reis FC, Abreu F, Marostica P, Rozov T, Cardieri J, Ludwing N, Valentin L, Rosario Filho NA, Camargo Neto E, Lewis E, Giugliani R, Diniz EMA, Culpi L, Phillip III JA, Chakraborty R. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients [Internet]. Journal of cystic fibrosis. 2008 ; 7( 1): 15-22.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.jcf.2007.03.006
Artigo de periodico
Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy (2008)
Kim, C. A.; Delépine, Marc; Boutet, Emilie; El Mourabit, Haquima; Lay, Soazig Le; Meier, Muriel; Nemani, Mona; Bridel, Etienne; Leite, Claudia C.; Bertola, Debora R.; Semple, Robert K.; O’Rahilly, Stephen; Dugail, Isabelle; Capeau, Jacqueline; Lathrop, Mark; Magre, Jocelyne
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: DISLIPIDEMIAS (PATOLOGIA), BIOLOGIA MOLECULAR, HIRSUTISMO (FISIOPATOLOGIA), TECIDO ADIPOSO (PATOLOGIA), IMAGEM POR RESSONÂNCIA MAGNÉTICA, FENÓTIPOS (ANÁLISE), MUTAÇÃO GENÉTICA, INSULINA (RESISTÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KIM, C. A. et al. Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy. Journal of Clinical Endocrinology and Metabolism, v. 93, n. 4, p. 1129-1134, 2008Tradução . . Disponível em: https://doi.org/10.1210/jc.2007-1328. Acesso em: 28 jun. 2024.
APA
Kim, C. A., Delépine, M., Boutet, E., El Mourabit, H., Lay, S. L., Meier, M., et al. (2008). Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy. Journal of Clinical Endocrinology and Metabolism, 93( 4), 1129-1134. doi:10.1210/jc.2007-1328
NLM
Kim CA, Delépine M, Boutet E, El Mourabit H, Lay SL, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O’Rahilly S, Dugail I, Capeau J, Lathrop M, Magre J. Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 4): 1129-1134.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2007-1328
Vancouver
Kim CA, Delépine M, Boutet E, El Mourabit H, Lay SL, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O’Rahilly S, Dugail I, Capeau J, Lathrop M, Magre J. Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 4): 1129-1134.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2007-1328
Artigo de periodico
The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency (2008)
Gomes, Larissa G.; Huang, Ningwu; Mendonça, Berenice B.; Bachega, Tania A. S. S.; Miller, Walter L.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: ENZIMAS OXIRREDUTORAS (VACINAÇÃO), HIDROXILASE (DEFICIÊNCIA), FENÓTIPOS, GENÓTIPOS, POLIMORFISMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Larissa G. et al. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 93, n. 7, p. 2913-2916, 2008Tradução . . Disponível em: https://doi.org/10.1210/jc.2008-0304. Acesso em: 28 jun. 2024.
APA
Gomes, L. G., Huang, N., Mendonça, B. B., Bachega, T. A. S. S., & Miller, W. L. (2008). The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency. Journal of Clinical Endocrinology and Metabolism, 93( 7), 2913-2916. doi:10.1210/jc.2008-0304
NLM
Gomes LG, Huang N, Mendonça BB, Bachega TASS, Miller WL. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 7): 2913-2916.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2008-0304
Vancouver
Gomes LG, Huang N, Mendonça BB, Bachega TASS, Miller WL. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 7): 2913-2916.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2008-0304
Artigo de periodico
Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment (2007)
Coutinho, Debora C.; Mendonça, Berenice B.; Coletta, Rocio R. D.; Costa, Elaine M. F.; Pachi, Paulo R.; Boguszewski, Margaret C. S.; Damiani, Durval; Arnhold, Ivo J. P.; Jorge, Alexander A. L.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: POLIMORFISMO, BIOLOGIA MOLECULAR, MUTAÇÃO GENÉTICA, NUCLEOTÍDEOS (ANÁLISE), CRESCIMENTO E DESENVOLVIMENTO (ESTUDO CLÍNICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COUTINHO, Debora C. et al. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment. Journal of Clinical Endocrinology and Metabolism, v. 92, n. 12, p. 4889-4892, 2007Tradução . . Disponível em: https://doi.org/10.1210/jc.2007-1661. Acesso em: 28 jun. 2024.
APA
Coutinho, D. C., Mendonça, B. B., Coletta, R. R. D., Costa, E. M. F., Pachi, P. R., Boguszewski, M. C. S., et al. (2007). Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment. Journal of Clinical Endocrinology and Metabolism, 92( 12), 4889-4892. doi:10.1210/jc.2007-1661
NLM
Coutinho DC, Mendonça BB, Coletta RRD, Costa EMF, Pachi PR, Boguszewski MCS, Damiani D, Arnhold IJP, Jorge AAL. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 12): 4889-4892.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2007-1661
Vancouver
Coutinho DC, Mendonça BB, Coletta RRD, Costa EMF, Pachi PR, Boguszewski MCS, Damiani D, Arnhold IJP, Jorge AAL. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 12): 4889-4892.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1210/jc.2007-1661
Artigo de periodico
Modulatory effects of the antioxidant ascorbic acid on the direct genotoxicity of doxorubicin in somatic cell of Drosophila melanogaster (2007)
Fragiorge, Edson José; Spanó, Mário Antonio; Antunes, Lusânia Maria Greggi
Source: Genetics and Molecular Biology. Unidade: FCFRP
Subjects: DROSOPHILA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRAGIORGE, Edson José e SPANÓ, Mário Antonio e ANTUNES, Lusânia Maria Greggi. Modulatory effects of the antioxidant ascorbic acid on the direct genotoxicity of doxorubicin in somatic cell of Drosophila melanogaster. Genetics and Molecular Biology, v. 30, n. 2, p. 449-455, 2007Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572007000300025. Acesso em: 28 jun. 2024.
APA
Fragiorge, E. J., Spanó, M. A., & Antunes, L. M. G. (2007). Modulatory effects of the antioxidant ascorbic acid on the direct genotoxicity of doxorubicin in somatic cell of Drosophila melanogaster. Genetics and Molecular Biology, 30( 2), 449-455. doi:10.1590/s1415-47572007000300025
NLM
Fragiorge EJ, Spanó MA, Antunes LMG. Modulatory effects of the antioxidant ascorbic acid on the direct genotoxicity of doxorubicin in somatic cell of Drosophila melanogaster [Internet]. Genetics and Molecular Biology. 2007 ; 30( 2): 449-455.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/s1415-47572007000300025
Vancouver
Fragiorge EJ, Spanó MA, Antunes LMG. Modulatory effects of the antioxidant ascorbic acid on the direct genotoxicity of doxorubicin in somatic cell of Drosophila melanogaster [Internet]. Genetics and Molecular Biology. 2007 ; 30( 2): 449-455.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1590/s1415-47572007000300025

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